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NCT Number: NCT06632080

Effects of Substance P on Headache Induction in Healthy Individuals

Substance P is a signaling molecule that has been implicated in the pathogenesis of headache. This study aims to ascertain whether administration of substance P can induce headache in healthy adults.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Danish Headache Center, Copenhagen University Hospital - Rigshospitalet

Glostrup Municipality, 2600, Denmark

Location contact

Hakan Ashina, MD, PhD

CONTACT

[email protected]

+45 28 10 24 95

About this study

Substance P is a vasoactive signaling molecule that belongs to the tachykinin family of peptides. It is expressed in multiple cells, including primary afferents of the trigeminal ganglion that innervate the meninges and its arteries. The best-known function of substance P is its role in pain transmission, and several lines of evidence has implicated substance P in the pathogenesis of headache. This study aims to ascertain whether intravenous infusion of substance P induces headache in healthy individuals who have no past or current history of primary or secondary headache disorder, except for infrequent episodic tension-type headache. For this purpose, we will conduct a randomized, double-blind, placebo-controlled, 2-way crossover trial.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 to 65 years of age upon entry into screening
  • A body weight of 50 to 100 kg
  • Provision of informed consent prior to initiation of any study-specific activities/procedures.

Exclusion criteria

  • Any history of a primary or secondary headache disorder, except for infrequent episodic tensiontype headache
  • Any first-degree relatives with a history of a primary headache disorder, except for infrequent episodic tension-type headache
  • Any history of moderate to severe traumatic brain injury
  • Any history of cardiovascular disease, including cerebrovascular diseases
  • Any history of pulmonary disease
  • Any other clinically significant disorders, conditions, or diseases that might impact the safety of the subject or interfere with the study's evaluation, procedures, or completion, aside from those mentioned above. This includes any relevant medical history or evidence that, in the opinion of the site investigator, might pose a risk to the subject or impact the validity of the study results
  • The subject is at risk of self-harm or harm to others as evidenced by past suicidal behavior
  • Female subjects of childbearing potential with a positive pregnancy test during any study visit
  • Cardiovascular disease of any kind, including cerebrovascular diseases
  • Hypertension (systolic blood pressure of ≥150 mmHg and/or diastolic blood pressure of ≥100 mmHg) prior to the start of infusion on the experimental day
  • Hypotension (systolic blood pressure of ≤90 mmHg and/or diastolic blood pressure of ≤50 mmHg)
  • Abnormalities on the electrocardiogram that, in the opinion of the site investigator, might pose a risk to the subject or impact the validity of the study results
  • Daily use of any medication other than contraceptives
  • Intake of any medication other than contraceptives within 48 hours of infusion start
  • Intake of caffeine, nicotine, and alcohol within 12 hours of infusion start
  • Headache of any intensity within 48 hours of infusion start

Treatment and study plan

Substance P

Drug

The participants will receive a continuous intravenous infusion of 20 mL of substance P (1.5 pmol/kg/min) over 20 minutes.

Placebo

Drug

The participants will receive a continuous intravenous infusion of 20 mL of placebo (isotonic saline) over 20 minutes.

Primary outcomes

  1. Incidence of Headache

    Time frame: 12 hours

    The primary outcome is the difference in the incidence of headache* between substance P and placebo during the 12-hour observational period after infusion start.

    • The intensity of headache is rated by the subject on the 11-point numerical rating scale (0 being no headache, 10 being the worst imaginable headache).

Secondary outcomes

  1. Headache Intensity Scores

    Time frame: 12 hours

    The secondary outcome is the difference in the area under the curve for median headache intensity scores between substance P and placebo during the 12-hour observational period after infusion start.

Other outcomes

  1. Dilation of the Superficial Temporal Artery

    Time frame: 2 hours

    The difference in area under the curve for relative STA dilation between substance P and placebo from the start of infusion to 2 hours after the infusion.

  2. Blood Flow Velocity in the Middle Cerebral Artery

    Time frame: 2 hours

    The difference in area under the curve for change in MCA mean blood flow velocity between substance P and placebo from the start of infusion to 2 hours after the infusion.

Study contacts

Contact information is provided by the study sponsor or research team.

Haidar Al-Khazali, MD

CONTACT

[email protected]

+45 41 59 84 94

Hakan Ashina, MD, PhD

CONTACT

[email protected]

+45 28 10 24 95

Sponsors and collaborators

Lead sponsor

Danish Headache Center

Other

Registry information

Official study title

Effects of Substance P on Headache Induction in Healthy Individuals: a Randomized Clinical Trial

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Oct 8, 2024
Registry last updated
Oct 15, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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